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2
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本文引用的文献

1
Monitoring CD8 T cell responses to NY-ESO-1: correlation of humoral and cellular immune responses.监测CD8 T细胞对NY-ESO-1的反应:体液免疫和细胞免疫反应的相关性
Proc Natl Acad Sci U S A. 2000 Apr 25;97(9):4760-5. doi: 10.1073/pnas.97.9.4760.
2
Phase I study in melanoma patients of a vaccine with peptide-pulsed dendritic cells generated in vitro from CD34(+) hematopoietic progenitor cells.一项针对黑色素瘤患者的I期研究,该研究使用了由CD34(+)造血祖细胞体外生成的肽脉冲树突状细胞疫苗。
Int J Cancer. 2000 May 1;86(3):385-92. doi: 10.1002/(sici)1097-0215(20000501)86:3<385::aid-ijc13>3.0.co;2-t.
3
A T-cell epitope determined with random peptide libraries and combinatorial peptide chemistry stimulates T cells specific for cutaneous T-cell lymphoma.用随机肽文库和组合肽化学方法确定的T细胞表位可刺激针对皮肤T细胞淋巴瘤的特异性T细胞。
Ann Oncol. 2000;11 Suppl 1:95-9.
4
Identification of NY-ESO-1 epitopes presented by human histocompatibility antigen (HLA)-DRB4*0101-0103 and recognized by CD4(+) T lymphocytes of patients with NY-ESO-1-expressing melanoma.鉴定由人类组织相容性抗原(HLA)-DRB4*0101-0103呈递、并被表达NY-ESO-1的黑色素瘤患者的CD4(+) T淋巴细胞识别的NY-ESO-1表位。
J Exp Med. 2000 Feb 21;191(4):625-30. doi: 10.1084/jem.191.4.625.
5
Stimulation of cytotoxic T cells against idiotype immunoglobulin of malignant lymphoma with protein-pulsed or idiotype-transduced dendritic cells.用蛋白脉冲或独特型转导的树突状细胞刺激细胞毒性T细胞对抗恶性淋巴瘤的独特型免疫球蛋白。
Blood. 2000 Feb 15;95(4):1342-9.
6
T-cell recognition of melanoma-associated antigens.T细胞对黑色素瘤相关抗原的识别。
J Cell Physiol. 2000 Mar;182(3):323-31. doi: 10.1002/(SICI)1097-4652(200003)182:3<323::AID-JCP2>3.0.CO;2-#.
7
Extracorporeal photopheresis in cutaneous T-cell lymphoma. Inconsistent data underline the need for randomized studies.体外光化学疗法治疗皮肤T细胞淋巴瘤。不一致的数据凸显了进行随机研究的必要性。
Br J Dermatol. 2000 Jan;142(1):16-21. doi: 10.1046/j.1365-2133.2000.03286.x.
8
Emerging new therapies for cutaneous T-cell lymphoma.皮肤T细胞淋巴瘤的新兴治疗方法。
Dermatol Clin. 2000 Jan;18(1):147-56. doi: 10.1016/s0733-8635(05)70155-8.
9
Five novel immunogenic antigens in meningioma: cloning, expression analysis, and chromosomal mapping.脑膜瘤中的五种新型免疫原性抗原:克隆、表达分析及染色体定位
Clin Cancer Res. 1999 Nov;5(11):3560-8.
10
Vaccination with mage-3A1 peptide-pulsed mature, monocyte-derived dendritic cells expands specific cytotoxic T cells and induces regression of some metastases in advanced stage IV melanoma.用mage-3A1肽脉冲处理的成熟单核细胞衍生树突状细胞进行疫苗接种,可扩增特异性细胞毒性T细胞,并诱导晚期IV期黑色素瘤的一些转移灶消退。
J Exp Med. 1999 Dec 6;190(11):1669-78. doi: 10.1084/jem.190.11.1669.

皮肤T细胞淋巴瘤相关抗原的血清学检测

Serological detection of cutaneous T-cell lymphoma-associated antigens.

作者信息

Eichmuller S, Usener D, Dummer R, Stein A, Thiel D, Schadendorf D

机构信息

German Cancer Research Center (DKFZ), Skin Cancer Unit (D0900), Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):629-34. doi: 10.1073/pnas.98.2.629. Epub 2001 Jan 9.

DOI:10.1073/pnas.98.2.629
PMID:11149944
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC14639/
Abstract

Cutaneous T-cell lymphomas (CTCL) are a group of skin neoplasms that originate from T lymphocytes and are difficult to treat in advanced stages. The present study is aimed at the identification of tumor-specific antigens from a human testis cDNA library using human sera known as the SEREX (serological identification of recombinantly expressed genes) approach. A cDNA library from normal testicle tissue was prepared and approximately 2 million recombinants were screened with sera from Sézary Syndrome and Mycosis fungoides patients. A total of 28 positive clones belonging to 15 different genes/ORFs were identified, including five hitherto unknown sequences. Whereas control sera did not react with most clones, 11-71% sera from CTCL patients were reactive against the identified clones. Expression analysis on 28 normal control and 17 CTCL tissues by reverse transcription-PCR (RT-PCR) and Northern blotting revealed seven ubiquitously distributed antigens, six differentially expressed antigens (several normal tissues were positive), and two tumor-specific antigens that were expressed only in testis and tumor tissues: (i) A SCP-1-like sequence, which has already been detected in various tumors, has been found in one CTCL tumor and four sera of CTCL patients reacted with various SCP-1-like clones and (ii) a new sequence named cTAGE-1 (CTCL-associated antigen 1) was detected in 35% of CTCL tumor tissues and sera of 6/18 patients reacted with this clone. The present study unravels CTCL-associated antigens independent of the T-cell receptor. The SCP-1-like gene and cTAGE-1 were shown to be immunogenic and immunologically tumor-specific and may therefore be candidates for immunotherapy targeting CTCL.

摘要

皮肤T细胞淋巴瘤(CTCL)是一组起源于T淋巴细胞的皮肤肿瘤,晚期难以治疗。本研究旨在使用称为SEREX(重组表达基因的血清学鉴定)的方法,从人睾丸cDNA文库中鉴定肿瘤特异性抗原。制备了来自正常睾丸组织的cDNA文库,并用来自Sezary综合征和蕈样肉芽肿患者的血清筛选了约200万个重组体。共鉴定出28个属于15个不同基因/开放阅读框的阳性克隆,包括5个迄今未知的序列。对照血清与大多数克隆无反应,而11%-71%的CTCL患者血清与鉴定出的克隆有反应。通过逆转录聚合酶链反应(RT-PCR)和Northern印迹对28个正常对照组织和17个CTCL组织进行表达分析,发现了7种普遍分布的抗原、6种差异表达的抗原(几种正常组织呈阳性)以及2种仅在睾丸和肿瘤组织中表达的肿瘤特异性抗原:(i)一种已在各种肿瘤中检测到的SCP-1样序列,在一个CTCL肿瘤中被发现,4份CTCL患者血清与各种SCP-1样克隆有反应;(ii)一种名为cTAGE-1(CTCL相关抗原1)的新序列在35%的CTCL肿瘤组织中被检测到,6/18患者的血清与该克隆有反应。本研究揭示了与CTCL相关的、独立于T细胞受体的抗原。SCP-1样基因和cTAGE-1被证明具有免疫原性且在免疫学上具有肿瘤特异性,因此可能是针对CTCL的免疫治疗候选物。